Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/60251
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dc.contributor.authorOrasa Pancharoenen_US
dc.contributor.authorAnan Athipornchaien_US
dc.contributor.authorAmpai Panthongen_US
dc.contributor.authorWalter Charles Tayloren_US
dc.date.accessioned2018-09-10T03:39:59Z-
dc.date.available2018-09-10T03:39:59Z-
dc.date.issued2008-06-01en_US
dc.identifier.issn13475223en_US
dc.identifier.issn00092363en_US
dc.identifier.other2-s2.0-45749126020en_US
dc.identifier.other10.1248/cpb.56.835en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=45749126020&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/60251-
dc.description.abstractA new isoflavone, 4′-γ,γ-dimethylallyloxy-5,7,2′, 5′-tetramethoxyisoflavone, brandisianin A (1), was isolated from the leaves of Millettia brandisiana, along with one synthetically known isoflavone, 7,4′-di-O-prenylgenistein (2) and twelve known compounds. The structures were elucidated on the basis of extensive spectroscopic analysis. Two isolated compounds were tested for anti-inflammatory activity; 12a-hydroxy-α- toxicarol (11) showed significant anti-inflammatory activity. © 2008 Pharmaceutical Society of Japan.en_US
dc.subjectChemistryen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleIsoflavones and rotenoids from the leaves of Millettia brandisianaen_US
dc.typeJournalen_US
article.title.sourcetitleChemical and Pharmaceutical Bulletinen_US
article.volume56en_US
article.stream.affiliationsSilpakorn Universityen_US
article.stream.affiliationsFaculty of Medicine, Chiang Mai Universityen_US
article.stream.affiliationsThe University of Sydneyen_US
Appears in Collections:CMUL: Journal Articles

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